Anti-reflective coating film

ABSTRACT

The present invention relates to an anti-reflective coating film. This anti-reflective coating film shows more improved interface adhesion and scratch resistance, which can be manufactured by a simple process.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of International Application No.PCT/KR2012/004764 filed Jun. 15, 2012, which claims priority to KoreanPatent Application No. 10-2011-0085787 filed on Aug. 26, 2011, KoreanPatent Application No. 10-2011-0085788 filed on Aug. 26, 2011, andKorean Patent Application No. 10-2012-0036337 filed on Apr. 6, 2012,which are incorporated herein in their entireties.

TECHNICAL FIELD

The present invention relates to an anti-reflective coating film.

BACKGROUND OF ART

In general, an anti-reflective film (anti-glare film) is disposed tominimize the reflection of external light on the screen of displaydevices such as PDP, CRT, and LCD.

The conventional anti-reflective coating film is commonly formed bydisposition of an anti-reflective layer on a light-transparentsubstrate. In this regard, the most widely used anti-reflective layerhas a three-layer structure of a hard coat layer and high and lowrefractive index layers sequentially laminated from thelight-transparent substrate. Recently, a two-layer structure omittingthe hard coat layer or the high refractive index layer from theanti-reflective layer has been commercialized, in order to simplify theproduction process. In order to provide anti-glare and scratch-resistantproperties, the anti-reflective coating film provided with an anti-glarehard coat layer has been also used.

Meanwhile, the anti-reflective coating film is commonly manufactured bya dry or wet method. Of the methods, the dry method is to laminate aplurality of thin layers using deposition or sputtering. This methodoffers superior adhesion at a layer interface, but requires highproduction cost, which is a limitation to commercial use.

In contrast, the wet method is to dry and cure a composition comprisinga binder, a solvent, etc., after applying it onto a substrate. Thismethod is less expensive than the dry method, and thus widely used incommercial applications. In the wet method, however, compositionsrequired for the formation of the hard coat layer and the high and lowrefractive index layers should be prepared separately, and each layer issequentially formed using the composition. Thus, the production processbecomes complicated, and offers weak adhesion at a film interface.

For this reason, many studies have been actively made to develop ananti-reflective coating composition capable of forming two or morelayers by a single wet coating process. However, there are still manyproblems that phase separation does not properly occur upon applying thecompositions during the production process, and thus individual layersdeteriorate in functions.

Further, the hard coat layer or the high refractive index layer istypically formed on the substrate as a pure binder or as a separatelayer comprising the binder and inorganic nanoparticles, and the hollowparticle-dispersed low refractive index layer is formed thereon.However, there are still problems that the anti-reflective coating filmhaving this structure has low durability because of weak adhesion at alayer interface.

DISCLOSURE OF INVENTION Technical Problem

The present invention provides an anti-reflective coating film showingmore improved interface adhesion and scratch resistance, which can bemanufactured by a simplified process.

Technical Solution

According to one embodiment of the present invention, provided is ananti-reflective coating film, comprising

a first layer that comprises a first (meth)acrylate-based binder andinorganic nanoparticles in the first (meth)acrylate-based binder, andthat has infiltrated into a substrate; and

a second layer that comprises a second (meth)acrylate-based binder andhollow particles in the second (meth)acrylate-based binder, and thatcovers the first layer,

in which a ratio of the cross-sectional area of the hollow particles toany cross-sectional area of the second layer is 70 to 95%.

In the anti-reflective coating film, the first (meth)acrylate-basedbinder may comprise a crosslinked polymer of a (meth)acrylate-basedcompound having a molecular weight of less than 600, and the second(meth)acrylate-based compound may comprise a crosslinked copolymer ofthe (meth)acrylate-based compound having a molecular weight of less than600 and a (meth)acrylate-based compound having a molecular weight of 600to 100,000.

Further, the first layer may further comprise the region having thecrosslinked copolymer of the (meth)acrylate-based compound having amolecular weight of less than 600 and the (meth)acrylate-based compoundhaving a molecular weight of 600 to 100,000, in addition to the regionhaving the crosslinked polymer. In this regard, the region having thecrosslinked copolymer may be located to a depth of approximately 5 to50% of the first layer, based on the interface between the first andsecond layers. Further, the crosslinked copolymer may be comprised toexhibit an increasing distribution gradient toward the second layer.

In the anti-reflective coating film of one embodiment, the second layermay further comprise inorganic nanoparticles.

Further, the (meth)acrylate-based compound having a molecular weight ofless than 600 may be one or more compounds selected from the groupconsisting of pentaerythritol tri(meth)acrylate, pentaerythritoltetra(meth)acrylate, dipentaerythritol hexa(meth)acrylate,trimethylenepropane tri(meth)acrylate, ethylene glycol di(meth)acrylate,9,9-bis[4-(2-acryloxyethoxy)phenyl]fluorene,bis(4-methacryloxythiophenyl)sulfide, and bis(4-vinylthiophenyl)sulfide.

Further, the second (meth)acrylate-based binder may comprise thecrosslinked copolymer further copolymerized with a fluorine-based(meth)acrylate compound, in addition to the (meth)acrylate-basedcompound having a molecular weight of less than 600 and the(meth)acrylate-based compound having a molecular weight of 600 to100,000.

Further, the (meth)acrylate-based compound having a molecular weight of600 to 100,000 may comprise a compound having two or more molecules ofthe (meth)acrylate-based compound having a molecular weight of less than600 linked via a linker, and the linker may comprise a urethane bond, athioether bond, an ether bond, or an ester bond. Further, the(meth)acrylate-based compound having a molecular weight of 600 to100,000 may have one or more substituents selected from the groupconsisting of an epoxy group, a hydroxyl group, a carboxyl group, athiol group, an aromatic or aliphatic hydrocarbon group having 6 carbonatoms or more, and an isocyanate group.

In the anti-reflective coating film of one embodiment, the inorganicnanoparticles may have a number average diameter of 5 to 50 nm, and forexample, they may be silica nanoparticles.

Further, the hollow particles may have a number average diameter of 5 to80 nm, and for example, they may be hollow silica particles.

Advantageous Effects

According to the present invention, two layers in an anti-reflectivecoating film can be formed by a single coating process, thereby formingthe anti-reflective coating film by a more simplified process. Further,the anti-reflective coating film thus formed is able to maintain moreimproved interface adhesion and scratch resistance and show an excellentanti-reflective effect, and thus it can be preferably used as ananti-reflective coating film in display devices, etc.

DESCRIPTION OF DRAWINGS

FIG. 1 is a schematic cross-sectional view showing a structure of ananti-reflective coating film according to one embodiment of the presentinvention;

FIG. 2 is a schematic flow chart showing a manufacturing method of ananti-reflective coating film according to one embodiment of the presentinvention; and

FIGS. 3 to 6 are microscopic images showing the cross-sections ofanti-reflective coating films according to Examples 1, 2, and 4 andComparative Example 1, respectively.

REFERENCE NUMERALS

-   -   1: Substrate    -   2: First layer (Hard coat layer)    -   3: Second layer (Low refractive index layer)    -   4: Hollow particles

BEST MODE FOR CARRYING OUT THE INVENTION

Hereinafter, an anti-reflective coating film and a manufacturing methodthereof according to embodiments of the present invention will bedescribed with reference to the accompanying drawings.

In advance, unless otherwise specified throughout the specification,several terms used herein are defined as follows.

First, the term ‘inorganic nanoparticle’ means a particle made fromvarious inorganic materials, and encompasses particles having a numberaverage diameter in nanometer scale, for example, a number averagediameter of 100 nm or less. These inorganic nanoparticles may beamorphous particles having substantially no void therein. For example,‘silica nanoparticles’ are particles made from a silicon compound or anorganic silicon compound, and means silicon compound particles ororganic silicon compound particles having a number average diameter of100 nm or less and substantially no void therein.

Further, the term ‘hollow particle’ means an organic or inorganicparticle having a void on the surface thereof and/or therein. Forexample, the term ‘hollow silica particle’ means a silica particle thatis made from a silicon compound or an organic silicon compound and has avoid on the surface of and/or inside the silica particle.

Further, the term ‘(meth)acrylate’ is defined to encompass acrylate andmethacrylate. The term ‘(meth)acrylate’ may be also defined to have nofluorine-containing substituent, and a compound having thefluorine-containing substituent may be referred to as a fluorine-based(meth)acrylate compound, in order to distinguish from each other.

Further, the term ‘coating layer’ means a composition layer formed byapplying (coating) the anti-reflective coating composition set forthbelow on a substrate film.

Further, the term ‘phase separation’ refers to the difference indistribution of a particular component from other components in thecomposition due to a difference in density, surface tension, or otherphysical properties of the components. Herein, when phase separation inthe coating occurs, at least two layers that can be distinguished areformed according to the distribution difference of a particularcomponent, for example, distribution difference of hollow particles.

Further, the phrase ‘infiltrated into the substrate’ means thatingredients for forming any layer of the anti-reflective coating film(for example, (meth)acrylate-based compound for forming a binder for thecorresponding layer and inorganic nanoparticles, etc) penetrate into thesubstrate to form the corresponding layer. For example, the ingredientsthat penetrate into the substrate are dried and cured so as to form aparticular layer in the region of the substrate into which they havepenetrated. In contrast, the phrase ‘a layer is formed on the substrate’means that the ingredients for forming the corresponding layersubstantially do not penetrate into the substrate, and they are driedand cured while forming an interface with the substrate, thereby forminga layer on the substarate without an overlapping region with thesubstrate by penetrating into the substrate.

Further, the phrase ‘a layer (e.g., the second layer of one embodimentof the present invention) covers the other layer (e.g., the first layerof that embodiment)’ means that there is substantially no distinctivelayer between the two layers. For example, in the anti-reflectivecoating film of one embodiment, ‘the second layer comprising hollowparticles covers the first layer that has infiltrated into thesubstrate’ means that there is substantially no separate and distinctivelayer between the first layer infiltrated into the substrate and thesecond layer comprising hollow particles, for example, substantially noseparate layer that has not infiltrated into the substrate and does notcomprise hollow particles. For example, in one embodiment, a separatelayer that comprises only the binder (e.g., crosslinked polymer formedfrom the (meth)acrylate-based compound) and/or inorganic nanoparticlesand that has not infiltrated into the substrate does not exist betweenthe first layer, that is, the infiltration layer and the second layercomprising hollow particles.

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Meanwhile, the present inventors have studied the anti-reflectivecoating film. As a result, they found that when the anti-reflectivecoating film is manufactured while inducing spontaneous phase separationusing a certain anti-reflective coating composition, the anti-reflectivecoating film shows more improved interface adhesion and scratchresistance and an excellent anti-reflective effect, thereby completingthe present invention. These excellent properties of the anti-reflectivecoating film are likely to be attributed to the specific structure ofthe film, in which the first layer serving as the hard coat layer hasinfiltrated into the substrate and the second layer serving as the lowrefractive index layer is formed to cover the first layer.

In contrast, the anti-reflective coating film having the structure offorming a separate hard coat layer comprising substantially no hollowparticles (e.g., a separate hard coat layer or high refractive indexlayer comprising the binder and substantially no hollow particles, oronly the binder and the inorganic nanoparticles) between the substrateand the low refractive index layer is disadvantageous in that additionalcoating or curing process is required for the formation of each layer,and thus the production process becomes complicated, or offers weakadhesion at a layer interface.

The anti-reflective coating film of one embodiment, in which the secondlayer (low refractive index layer) covers the first layer (hard coatlayer) that has infiltrated into the substrate, shows excellentinterface adhesion, even though formed by a simple process of a singlecoating and curing process.

The anti-reflective coating film of one embodiment may comprise thefirst layer that comprises the first (meth)acrylate-based binder andinorganic nanoparticles in the first (meth)acrylate-based binder, andthat has infiltrated into the substrate; and the second layer thatcomprises the second (meth)acrylate-based binder and hollow particles inthe second (meth)acrylate-based binder, and that covers the first layer.In the anti-reflective coating film, a ratio of the cross-sectional areaof the hollow particles to any cross-sectional area of the second layermay be approximately 70 to 95%, or approximately 75 to 93%, orapproximately 80 to 90%, or approximately 85 to 92%.

In the anti-reflective coating film, the first layer infiltrated intothe substrate may serve as the hard coat layer of the anti-reflectivecoating film, and also as the high refractive index layer showing arefractive index of approximately 1.5 or more. The first(meth)acrylate-based binder infiltrated into the substrate is comprisedin the hard coat layer, and the first (meth)acrylate-based binder maycomprise the crosslinked polymer of the (meth)acrylate-based compoundhaving a molecular weight of less than 600. In addition, the hard coatlayer may comprise inorganic nanoparticles in the first(meth)acrylate-based binder.

Further, in the second layer that is in contact with and covers thefirst layer as the infiltration layer in the substrate, all or most(e.g., approximately 97% by weight or more, or approximately 99% byweight or more) of the hollow particles are substantially distributed,and thus the second layer functions as the low refractive index layer ofthe anti-reflective coating film. This low refractive index layer showsa low refractive index of approximately 1.45 or less, thereby exhibitingproper anti-reflective effect. The low refractive index layer comprisesthe second (meth)acrylate-based binder, which may comprise thecrosslinked copolymer of the (meth)acrylate-based compound having amolecular weight of less than 600 and the (meth)acrylate-based compoundhaving a molecular weight of 600 to 100,000. The low refractive indexlayer may also comprise the hollow particles in the second(meth)acrylate-based binder.

In the anti-reflective coating film, the first (meth)acrylate-basedbinder of the first layer serving as the hard coat layer may furthercomprise the crosslinked copolymer of the (meth)acrylate-based compoundhaving a molecular weight of less than 600 and the (meth)acrylate-basedcompound having a molecular weight of 600 to 100,000. The second layerserving as the low refractive index layer may further comprise theinorganic nanoparticles.

FIG. 1 is a schematic cross-sectional view showing the anti-reflectivecoating film according to an exemplary embodiment. With reference toFIG. 1, in the anti-reflective coating film, the first layer 2 servingas the hard coat layer is infiltrated into the substrate 1, and curedtherein, and the second layer 3 serving as the low refractive indexlayer is formed on the substrate by contacting with and covering thefirst layer 2 as the infiltration layer. In this regard, there is noseparate layer between the first layer 2 infiltrated into the substrateand the second layer 3 on the substrate, which means that a separatelayer, for example, comprising only the binder and/or the inorganicnanoparticles and substantially no hollow particles and without havinginfiltrated into the substrate does not exist between the first layer asthe infiltration layer and the second layer substantially having hollowparticles.

As the first layer 2 serving as the hard coat layer has infiltrated intothe substrate 1, and the second layer 3 serving as the low refractiveindex layer is formed to be in contact therewith, the anti-reflectivecoating film of another embodiment has excellent interface adhesionbetween the substrate, hard coat layer and low refractive index layer,and therefore, delamination can be minimized during use.

Further, a ratio of the cross-sectional area of the hollow particles toany cross-sectional area of the second layer is made to be approximately70 to 95%, or approximately 75 to 93%, or approximately 80 to 90%, orapproximately 85 to 92%, and thus the hollow particles can be compactlydistributed in the second layer serving as the low refractive indexlayer. Therefore, the anti-reflective coating film of one embodimentexhibits excellent low refractive index property and anti-reflectiveeffect.

Hereinafter, individual layers comprised in the anti-reflective coatingfilm will be described in more detail.

First, the anti-reflective coating film comprises the substrate. Asshown in FIG. 1, the substrate 1 is a typical transparent thin film, andany material may be used without limitation, as long as it can beinfiltrated with the first (meth)acrylate-based binder of the firstlayer and the inorganic nanoparticles. For example, the substrate may bemade from polyester-based resins, polycarbonate-based resins,acrylic-based resins, acetate cellulose resins or the like. In oneembodiment, a triacetate cellulose (TAC) resin may be used as thesubstrate in order to improve transparency and anti-reflective effect.

Further, the anti-reflective coating film may comprise the first layer 2serving as the hard coat layer, which comprises the crosslinked polymerof the (meth)acrylate-based compound having a molecular weight of lessthan 600 as the first (meth)acrylate-based binder, and the inorganicnanoparticles in the first (meth)acrylate-based binder. The hard coatlayer may be a layer infiltrated into the substrate. The first layer 2may be cured and integrated into the substrate by infiltration of thefirst (meth)acrylate-based binder and the inorganic nanoparticles intothe substrate. Even though FIG. 1 shows infiltration of the first layer2 into the entire surface of the substrate 1, the first layer 2 mayinfiltrate into a part of the substrate 1 in another embodiment.

The second layer 3 serving as the low refractive index layer is formedto be in contact with and cover the first layer 2 that has infiltratedinto the substrate 1, and it may be a layer containing hollow particles.More particularly, a separate layer containing only the binder and/orinorganic nanoparticles and having not infiltrated into the substratedoes not exist between the first layer 2 and the second layer 3. As inthe case of the known films, a separate layer comprising only the binderexists between the hard coat layer and the low refractive index layerresults in a disadvantage of reducing adhesion between each layer andthe substrate. In contrast, the anti-reflective coating film of oneembodiment is formed such that the second layer 3 serving as the lowrefractive index layer is in contact with the substrate 1 and the firstlayer 2 serving as the hard coat layer, thereby showing more improvedinterface adhesion, scratch resistance, and anti-reflective effect.

Herein, the second (meth)acrylate-based binder of the second layer 3 maycomprise the crosslinked copolymer of the (meth)acrylate-based compoundhaving a molecular weight of less than 600 and the (meth)acrylate-basedcompound having a molecular weight of 600 to 100,000. In anotherembodiment, the second (meth)acrylate-based binder may comprise thecrosslinked copolymer of the (meth)acrylate-based compound having amolecular weight of less than 600, the (meth)acrylate-based compoundhaving a molecular weight of 600 to 100,000 and the fluorine-based(meth)acrylate compound. As the crosslinked copolymer prepared byfurther copolymerizing with the fluorine-based (meth)acrylate compoundis comprised in the second (meth)acrylate-based binder, the second layer3 serving as the low refractive index layer shows a lower refractiveindex and excellent anti-reflective effect. In addition, the scratchresistance of the second layer 3 can be more improved.

In addition, the second layer 3 may further comprise the inorganicnanoparticles in the second (meth)acrylate-based binder, thereby moreimproving the scratch resistance and anti-reflective effect of thesecond layer 3.

Meanwhile, the first (meth)acrylate-based binder of the first layer 2may further comprise the crosslinked copolymer of the(meth)acrylate-based compound having a molecular weight of less than 600and the (meth)acrylate-based compound having a molecular weight of 600to 100,000, in addition to the crosslinked polymer of the abovementioned (meth)acrylate-based compound having a molecular weight ofless than 600.

In this regard, the crosslinked copolymer in the first(meth)acrylate-based binder of the first layer 2 may be comprised in thecertain region of the first layer 2, based on the interface between thefirst layer 2 and the second layer 3, for example, to approximately 5 to50% depth, or approximately 5 to 45% depth, or approximately 5 to 40%depth of the first layer 2. The crosslinked copolymer in the binder ofthe first layer 2 may be comprised to exhibit an increasing distributiongradient toward the second layer 3.

As such, the (meth)acrylate-based compound having a molecular weight of600 to 100,000 is crosslinked copolymerized with the(meth)acrylate-based compound having a molecular weight of less than 600with distribution gradient to the predetermined depth of the first layer2, and the crosslinked copolymers are also comprised throughout thesecond layer 3. Therefore, the interface adhesion between the firstlayer 2 and the second layer 3 can be more improved, and hollowparticles comprised in the second layer 3 can be more compactlydistributed.

In the above mentioned anti-reflective coating film, the first layer 2is a layer having a higher refractive index than the second layer 3serving as the low refractive index layer, and the refractive index maybe approximately 1.5 to 1.58, or approximately 1.5 to 1.57, orapproximately 1.51 to 1.56. In addition, the second layer 3 may have arefractive index of approximately 1.1 to 1.45, or approximately 1.15 to1.43, or approximately 1.2 to 1.42.

In addition, the anti-reflective coating film according to anotherembodiment has a reflectance of approximately 0.5 to 4%, orapproximately 0.8 to 3%, or approximately 1 to 2% to show excellentanti-reflective properties, and thus it can be properly used as theanti-reflective coating film in various display devices such as PDP, CRTor LCD.

Hereinafter, the anti-reflective coating composition for forming theanti-reflective coating film of one embodiment and the method formanufacturing the anti-reflective coating film using the same will bedescribed.

The anti-reflective coating composition may comprise the(meth)acrylate-based compound having a molecular weight of less than600; the (meth)acrylate-based compound having a molecular weight of 600to 100,000; inorganic nanoparticles; and hollow particles. Eachcomponent of the composition will be described as follows.

(Meth)acrylate-Based Compound Having Molecular Weight of Less than 600

First, the anti-reflective coating composition may comprise the(meth)acrylate-based compound having a molecular weight of less than600. If the composition is applied to any substrate, at least a part ofthe (meth)acrylate-based compound having a low molecular weight mayinfiltrate into the substrate.

The low molecular weight-(meth)acrylate-based compound infiltrated intothe substrate may be polymerized alone or copolymerized with the highmolecular weight-(meth)acrylate-based compound explained below andhaving a molecular weight of 600 to 100,000 to form a binder of thefirst layer corresponding to the infiltrated region.

The residual low molecular weight-(meth)acrylate-based compound mayremain on the substrate without infiltrating into the substrate. Theresidual compound is copolymerized with the high molecularweight-(meth)acrylate-based compound explained below to form a binder ofthe second layer that covers the first layer formed in the infiltratedregion of the substrate.

In order to sufficiently infiltrate the low molecularweight-(meth)acrylate-based compound into the substrate and to form thebinder of the first layer serving as the hard coat layer of theanti-reflective coating film, the low molecularweight-(meth)acrylate-based compound may have, for example, a molecularweight of less than approximately 600, or less than approximately 500,or less than approximately 400, and in another embodiment, it may have amolecular weight of approximately 50 or more, or approximately 100 ormore.

In exemplary embodiment, in order to form the first layer that hasinfiltrated into the substrate to show higher refractive index (e.g.,hard coat layer and/or high refractive index layer), the low molecularweight-(meth)acrylate-based compound may have a substituent such assulfur, chlorine or metal, or an aromatic substituent.

The low molecular weight-(meth)acrylate-based compound may comprise acompound selected from the group consisting of pentaerythritoltri(meth)acrylate, pentaerythritol tetra(meth)acrylate,dipentaerythritol hexa(meth)acrylate, trimethylenepropanetri(meth)acrylate, ethylene glycol di(meth)acrylate,9,9-bis(4-(2-acryloxyethoxyphenyl)fluorine (refractive index: 1.62),bis(4-methacryloxythiophenyl)sulfide (refractive index: 1.689), andbis(4-vinylthiophenyl)sulfide (refractive index: 1.695), or a mixture oftwo or more thereof.

(Meth)acrylate-Based Compound Having Molecular Weight of 600 to 100,000

Meanwhile, the anti-reflective coating composition may comprise the highmolecular weight-(meth)acrylate-based compound having a molecular weightof 600 to 100,000. When the composition is applied to any substrate, arelatively smaller amount of the high molecularweight-(meth)acrylate-based compound may infiltrate into the substrate,compared to the above mentioned low molecular weight-compound, and therest thereof may remain on the substrate, due to its high molecularweight and bulky chemical structure.

Therefore, the high molecular weight-(meth)acrylate-based compound doesnot infiltrate into the substrate to a depth equivalent to that of theabove mentioned low molecular weight-(meth)acrylate-based compound. As aresult, the infiltrated region of the substrate may be divided into thefollowing two regions. First, in the region infiltrated with only thelow molecular weight-(meth)acrylate-based compound or in the region at adepth to be infiltrated therewith, a binder formed from a crosslinkedpolymer of the low molecular weight-(meth)acrylate-based compound mayexist. In the other infiltrated region that is infiltrated with the highmolecular weight-(meth)acrylate-based compound, the crosslinkedcopolymer of the high molecular weight-(meth)acrylate-based compound andthe low molecular weight-(meth)acrylate-based compound may exist as thebinder.

The residual high molecular weight-(meth)acrylate-based compound thathas not infiltrated into the substrate may be copolymerized with theabove mentioned low molecular weight-(meth)acrylate-based compound toform a second (meth)acrylate-based binder of the second layer (e.g., lowrefractive index layer of anti-reflective coating film) covering theinfiltration layer. Therefore, interface adhesion between the firstlayer serving as the hard coat layer of the anti-reflective coating filmand the second layer covering thereon (low refractive index layer) isimproved, scratch resistance of the low refractive index layer is alsoimproved, and hollow particles in the low refractive index layer aremore compactly dispersed.

The high molecular weight-(meth)acrylate-based compound is a compoundhaving a higher molecular weight than the above mentioned low molecularweight-compound and a bulky structure. For example, it may have amolecular weight of approximately 400 or more, or approximately 500 ormore, or approximately 600 or more. For another example, it may have amolecular weight of approximately 100,000 or less, or approximately80,000 or less, or approximately 50,000 or less.

For the high molecular weight and bulky structure, the high molecularweight-(meth)acrylate-based compound may comprise a compound having astructure of linking two or more molecules of the above mentioned lowmolecular weight-(meth)acrylate-based compound via a linker. In thisregard, the linker may be any chemical bond known to link the(meth)acrylate-based compounds, and for example, a divalent orhigher-valent radical comprising a urethane bond, a thioether bond, anether bond or an ester bond.

For more bulky structure, the high molecular weight-(meth)acrylate-basedcompound may also have one or more substituents selected from the groupconsisting of an epoxy group, a hydroxyl group, a carboxyl group, athiol group, an aromatic or aliphatic hydrocarbon group having 6 carbonatoms or more, and an isocyanate group.

The high molecular weight-(meth)acrylate-based compound may be acommercially available product satisfying the above conditions ordirectly synthesized. Examples of the commercially available product maycomprise UA-306T, UA-306I, UA-306H, UA-510T, UA-510I, and UA-510H(products of KYOEISHA Co.); BPZA-66 and BPZA-100 (products of KYOEISHACo.); EB9260 and EB9970 (products of BAEYER Co.); and Miramer SP1107 andMiramer SP1114 (products of MIWON Co.).

The above mentioned high molecular weight-(meth)acrylate-based compoundmay be comprised in the anti-reflective coating composition in an amountof approximately 5 to 30 parts by weight, or approximately 5 to 25 partsby weight, or approximately 5 to 20 parts by weight, based on 100 partsby weight of the low molecular weight-(meth)acrylate-based compound. Thecontent of the high molecular weight-(meth)acrylate-based compound maybe determined, considering optimization of physical properties of thelayer or changes in the distribution of hollow particles according toaddition of an excessive amount thereof as well as minimal effectsachieved by use of the binder compositions comprising the high and lowmolecular weight-(meth)acrylate-based compounds.

Fluorine-Based (Meth)Acrylate Compound

Meanwhile, the above mentioned anti-reflective coating composition mayfurther comprise the fluorine-based (meth)acrylate compound substitutedwith one or more fluorine atoms as the binder composition. Owing to thepresence of the fluorine-containing substituent, the fluorine-based(meth)acrylate compound does not infiltrate into the substrate when thecomposition is applied to the substrate. For this reason, thefluorine-based (meth)acrylate compound may form the second(meth)acrylate-based binder of the second layer that serves as the lowrefractive index layer of the anti-reflective coating film, togetherwith the above mentioned low and high molecular weight-(meth)acrylatecompounds. The fluorine-based (meth)acrylate compound shows a lowerrefractive index, thereby reducing the refractive index of the lowrefractive index layer and showing excellent compatibility with theafter-mentioned hollow particles due to polar functional groups, andalso improving scratch resistance of the low refractive index layer.

The fluorine-based (meth)acrylate compound may have a structure oflinking one or more fluorine-containing substituents to any(meth)acrylate compound, and examples of the fluorine-based(meth)acrylate compound may be one or more compounds selected from thegroup consisting of the compounds of the following Chemical Formulae 1to 5:

wherein R¹ is a hydrogen group or an alkyl group having 1 to 6 carbonatoms, a is an integer of 0 to 7, and b is an integer of 1 to 3;

wherein c is an integer of 1 to 10;

wherein d is an integer of 1 to 11;

wherein e is an integer of 1 to 5;

wherein f is an integer of 4 to 10.

Meanwhile, the fluorine-based (meth)acrylate compound may be comprisedin the anti-reflective coating composition in an amount of approximately0.5 to 20 parts by weight, or approximately 5 to 18 parts by weight, orapproximately 10 to 16 parts by weight, based on 100 parts by weight ofthe above mentioned low molecular weight-(meth)acrylate compound.

The fluorine-based (meth)acrylate compound may be a commerciallyavailable product satisfying the above conditions. Examples of thecommercially available product may comprise OPTOOL AR110 (manufacturedby DAIKIN), LINC-3A and LINC-102A (manufactured by KYOEISHA), PFOA(manufactured by Exfluor), and OP-38Z (manufactured by DIC).

Inorganic Nanoparticles

Meanwhile, inorganic nanoparticles may be comprised in theanti-reflective coating composition.

A part of the inorganic nanoparticles may infiltrate into and bedispersed in the substrate, together with the above mentioned two ormore binder compositions, when the composition is applied to asubstrate. The remainer thereof that has not infiltrated into thesubstrate is dispersed in the second layer serving as the low refractiveindex layer, and contributes to the improvement of scratch resistanceand anti-reflective effect.

In one embodiment, the inorganic nanoparticles may be particles that aremade from various inorganic materials and have a number average diameterof nanometer scale.

These inorganic nanoparticles may have a number average diameter of, forexample, approximately 100 nm or less, or approximately 5 to 50 nm, orapproximately 5 to 20 nm. To control transparency, refractive index, andscratch resistance of the coating layer, the diameter of the inorganicnanoparticles should be controlled within the above range.

Further, to obtain improved transparency of the coating layer on thesubstrate, the silica nanoparticles made from the silicon compound ororganic silicon compound may be used as inorganic nanoparticles.

The inorganic nanoparticles may be comprised in the anti-reflectivecoating composition in an amount of, for example, approximately 5 to 30parts by weight, or approximately 5 to 25 parts by weight, orapproximately 5 to 20 parts by weight, based on 100 parts by weight ofthe above mentioned low molecular weight-(meth)acrylate-based compound.The content of the inorganic nanoparticles may be controlled within theabove range, considering the infiltration content of inorganicnanoparticles according to the type of substrate and a reduction ofanti-reflective effect by increased reflectance resulting from additionof an excessive amount thereof as well as the minimal effect of theinorganic nanoparticles.

Meanwhile, the inorganic nanoparticles are dispersed in a dispersionmedium, and may be comprised in the form of sol having a solid contentof approximately 5 to 40% by weight. Herein, examples of the organicsolvent to be used as the dispersion medium may comprise alcohols suchas methanol, isopropyl alcohol (IPA), ethylene glycol, and butanol;ketones such as methyl ethyl ketone (MEK) and methyl isobutyl ketone(MIBK); aromatic hydrocarbons such as toluene and xylene; amides such asdimethyl formamide, dimethyl acetamide, and N-methylpyrrolidone; esterssuch as ethyl acetate, butyl acetate, and γ-butyrolactone; ethers suchas tetrahydrofuran and 1,4-dioxane; or mixtures thereof.

According to one embodiment, commercially available silica sol may beused as the inorganic particles, and exemplified by MEK-ST, MIBK-ST,MIBK-SD, MIBK-SD-L, MEK-AC, DMAC-ST, and EG-ST manufactured by Nissanchemical Co.; or Purisol manufactured by Gaematech Co.

Hollow Particles

Meanwhile, hollow particles may be further comprised in theanti-reflective coating composition. These hollow particles meanparticles having voids on the surface of and/or inside the particles,and are an ingredient for achieving low refractive index andanti-reflective effect.

These hollow particles, when the composition is applied to thesubstrate, are substantially not distributed in the first layer thatserves as the hard coat layer of the anti-reflective coating film, andthey are substantially distributed in the layer covering the firstlayer, that is, in the second layer serving as the low refractive indexlayer. Herein, the hollow particles “substantially not distributed(comprised)” in the first layer mean that the content of the hollowparticles present in the first layer serving as the infiltration layerin the substrate is less than approximately 5% by weight, or less thanapproximately 3% by weight, or less than approximately 1% by weight,based on the total weight of the hollow particles.

Meanwhile, a solvent is comprised in the composition of one embodiment,together with the above mentioned binder composition, etc., andtherefore, spontaneous phase separation occurs to form theanti-reflective coating film. At this time, when phase separationoccurs, the hollow particles are substantially not distributed in thefirst layer as the infiltration layer due to the difference in thedensity or in surface energy between the hollow particles and othercomponents, and they are compactly distributed in the second layerserving as the low refractive index layer. As a result, it is possibleto form the anti-reflective coating film showing more improved filmstrength, scratch resistance and anti-reflective property.

The material of these hollow particles is not particularly limited, aslong as it is in the form of particles having voids on the surface ofand/or inside the particles. In one embodiment, in order to provide thelow refractive index layer with transparency and/or low refractiveindex, hollow silica particles generated from the silicon compound ororganic silicon compound may be used.

At this time, the diameter of the hollow particles may be determinedwithin the range of maintaining transparency of the film and showinganti-reflective effect. For example, the hollow particles may have anumber average diameter of approximately 5 to 80 nm, or approximately 10to 75 nm, or approximately 20 to 70 nm.

The hollow particles may be comprised in the anti-reflective coatingcomposition in an amount of approximately 1 to 30 parts by weight, orapproximately 1 to 25 parts by weight, or approximately 5 to 20 parts byweight, based on 100 parts by weight of the above mentioned lowmolecular weight-(meth)acrylate-based compound. In order to achievetheir minimal effect of hollow particles and formation of theirpreferred distribution by phase separation, the content of the hollowparticles may be controlled within the above mentioned range.

Further, the hollow particles may be dispersed in a dispersion medium(water or organic solvent), and comprised in the form of colloid havinga solid content of approximately 5 to 40% by weight. Herein, examples ofthe organic solvent to be used as the dispersion medium may comprisealcohols such as methanol, isopropyl alcohol (IPA), ethylene glycol, andbutanol; ketones such as methyl ethyl ketone (MEK) and methyl isobutylketone (MIBK); aromatic hydrocarbons such as toluene and xylene; amidessuch as dimethyl formamide, dimethyl acetamide, and N-methylpyrrolidone;esters such as ethyl acetate, butyl acetate, and γ-butyrolactone; etherssuch as tetrahydrofuran and 1,4-dioxane; or mixtures thereof.

Solvent

A solvent may be further comprised in the above mentionedanti-reflective coating composition. The solvent functions to controlinfiltration of the binder compositions into the substrate and the phaseseparation and distribution pattern of hollow particles as well as theviscosity of the composition within the proper range.

In order to achieve the above effects, the solvent may be a solventhaving a dielectric constant (25° C.) of approximately 20 to 30 and adipole moment of approximately 1.7 to 2.8. Examples of the solventcapable of satisfying these physical properties may comprise methylethyl ketone, ethyl acetate, acetyl acetone or the like, and any solventcapable of satisfying the physical properties can be also used.According to one embodiment, other solvent may be also mixed, togetherwith the solvent capable of satisfying the physical properties. Examplesof the solvent to be mixed may comprise isobutyl ketone, methanol,ethanol, n-butanol, i-butanol, t-butanol or the like. However, in termsof proper phase separation, it is preferable that the solvent satisfyingthe range of the dielectric constant and dipole moment is comprised inan amount of approximately 60% by weight or more, based on the totalweight of the solvent comprised in the composition.

In the anti-reflective coating composition, the solvent may be comprisedin an amount of, for example, approximately 100 to 500 parts by weight,or approximately 100 to 450 parts by weight, or approximately 100 to 400parts by weight, based on 100 parts by weight of the above mentioned lowmolecular weight-(meth)acrylate-based compound. If the composition showsbad flowability upon coating, defects such as stripes on the coatinglayer may be generated. In order to provide the composition with theminimum flowability required, the solvent may be comprised in thepredetermined content or more. When an excessive amount of the solventis added, the solid content becomes too low, and therefore, defects maybe generated upon drying and curing, and the distribution of the hollowparticles may be deviated from the preferred range.

Initiator

Meanwhile, an initiator may be further comprised in the above mentionedanti-reflective coating composition. The initiator is a compound that isactivated by energy ray such as ultraviolet ray so as to inducepolymerization of the binder compositions. A compound typically used inthe art may be used.

Examples of the initiator may comprise 1-hydroxy cyclohexylphenylketone, benzyl dimethyl ketal, hydroxy dimethyl acetophenone, benzoin,benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether orbenzoin butyl ether, and various other photoinitiators.

At this time, the content of the initiator may be, for example,approximately 5 to 25 parts by weight, or approximately 5 to 20 parts byweight, or approximately 5 to 15 parts by weight, based on 100 parts byweight of the low molecular weight-(meth)acrylate-based compound. Forsufficient polymerization of the binder compositions, the initiator maybe comprised in the predetermined content or more. When an excessiveamount of the initiator is added, each layer constituting theanti-reflective coating film may have the reduced mechanical propertiessuch as scratch resistance or abrasion resistance.

Next, the method for manufacturing the anti-reflective coating filmusing the above mentioned anti-reflective coating composition will bedescribed. FIG. 2 is a schematic flow chart showing the manufacturingmethod of one embodiment, in which the anti-reflective coating film ismanufactured using the above mentioned anti-reflective coatingcomposition.

With reference to FIG. 2, the method for manufacturing theanti-reflective coating film comprises the steps of preparing the abovementioned anti-reflective coating composition; applying it onto at leastone surface of the substrate; drying the composition to allow a part ofthe binder composition and inorganic nanoparticles to infilterate intothe substrate; and curing the infiltrated and dried composition to formthe first layer corresponding to the infiltrated region of thesubstrate, and the second layer that contains hollow particles andcovers the first layer.

Through the manufacturing method, the solvent having certain physicalproperties in the composition may first dissolve a part of thesubstrate, and subsequently, parts of the binder compositions (e.g.,parts of the (meth)acrylate-based compounds having low and highmolecular weights) and at least a part of the inorganic nanoparticlesmay infiltrate into the substrate. At this time, the remainder of thebinder compositions and the inorganic nanoparticles that has notinfiltrated, and the hollow particles may form the coating layer (e.g.,second layer) on the substrate. In particular, this coating layer mayremain as a thin layer on the substrate that is infiltrated with theabove components, and the hollow particles may compactly exist insidethe coating layer.

Thereafter, when a curing process is performed, the first and second(meth)acrylate-based binders of the first and second layers are formed,and the first layer serving as the hard coat layer may be formed as aninfiltration layer inside the substrate and the second layer containingthe hollow particles may be formed to cover the first layer. As aresult, the anti-reflective coating film of one embodiment can bemanufactured.

As described above, even though a single coating and curing process isapplied using a single composition, the anti-reflective coating film ofone embodiment can be manufactured by a simple process owing toinfiltration of parts of the components into the substrate and phaseseparation. In this anti-reflective coating film, in particular, thefirst layer serving as the hard coat layer has infiltrated into thesubstrate to be in contact with the second layer, thereby showingexcellent interface adhesion and mechanical properties. In thisanti-reflective coating film, furthermore, a separate layer does notexist between the first and second layers, and hollow particles arecompactly present in the second layer, thereby showing lower refractiveindex and excellent anti-reflective property. As the above mentionedanti-reflective coating composition comprises at least two types of the(meth)acrylate-based compounds having different molecular weights andthe solvent having the predetermined physical properties, infiltrationinto the substrate and phase separation can be optimized.

In the method for manufacturing the above anti-reflective coating film,the method of applying the composition onto at least one surface of thesubstrate may be performed using a coating apparatus and methodtypically used in the art, such as wire bar.

Further, the drying process may be performed at the temperature ofapproximately 5 to 150° C. for approximately 0.1 to 60 minutes,approximately 20 to 120° C. for approximately 0.1 to 20 minutes, orapproximately 30 to 110° C. for approximately 1 to 10 minutes, in orderto facilitate phase separation of the composition and infiltration ofthe composition into the substrate.

Further, in the curing process, polymerization is initiated by applyingenergy to the dried composition such as photoradiation, thereby curingthe infiltrated and dried composition. In the curing process, UVradiation may be performed at approximately 0.1 to 2 J/cm² forapproximately 1 to 600 seconds, or approximately 0.1 to 1.5 J/cm² forapproximately 2 to 200 seconds, or approximately 0.2 to 1 J/cm² forapproximately 3 to 100 seconds, in order to induce sufficient curingreaction.

Through this method, the above mentioned anti-reflective coating film ofone embodiment can be obtained, in which a ratio of the cross-sectionalarea of the hollow particles to any cross-sectional area of the secondlayer serving as the low refractive index layer is made to beapproximately 70 to 95%, or approximately 75 to 93%, or approximately 80to 90%, or approximately 85 to 92%, and thus the hollow particles can becompactly distributed in the low refractive index layer.

It is apparent that the method for manufacturing the anti-reflectivecoating film further comprises the steps typically performed in the artbefore or after each step, in addition to the above described steps.

Hereinafter, preferred Examples of the present invention will bedescribed for better understanding. However, the following Examples aregiven for illustrative purposes only, and are not intended to limit thepresent invention.

Example 1 Preparation of Anti-Reflective Coating Composition

Based on 100 parts by weight of a (meth)acrylate-based compoundcomprising 100 parts by weight of pentaerythritol hexaacrylate(molecular weight: 298.3) and 11.33 parts by weight of acrylate having aurethane functional group (manufactured by KYOEISHA, product name:UA-306T, molecular weight: 1000);

approximately 15.87 parts by weight of silica nanoparticle-dispersedsilica sol (dispersion medium: methyl isobutyl ketone and methylalcohol, solid content: 40% by weight, number average diameter of silicananoparticles: 10 nm, manufactured by Gaematech, product name: Purisol);

approximately 11.33 parts by weight of a hollow silica-dispersedcolloidal solution (dispersion medium: methyl isobutyl ketone, solidcontent: 20% by weight, number average diameter of hollow silica: 50 nm,manufactured by Catalysts & Chemicals Industries Co., product name:MIBK-sol);

approximately 10.85 parts by weight of a photoinitiator (specifically,approximately 1.11 parts by weight of Darocur-1173, approximately 6.48parts by weight of Irgacure-184, approximately 2.15 parts by weight ofIrgacure-819, and approximately 1.11 parts by weight of Irgacure-907);and

approximately 251.85 parts by weight of a solvent (specifically,approximately 179.63 parts by weight of methyl ethyl ketone (MEK),approximately 24.07 parts by weight of ethanol, approximately 24.07parts by weight of n-butyl alcohol and approximately 24.07 parts byweight of acetyl acetone) were mixed to prepare an anti-reflectivecoating composition.

(Manufacturing of Anti-Reflective Coating Film)

The anti-reflective coating composition was applied to a triacetatecellulose film (thickness of 80 μm) using a wire bar (No. 9). The filmwas dried in a 90° C. oven for 1 minute, and then UV energy of 200mJ/cm² was irradiated thereto for 5 seconds to cure the composition.

Finally, an anti-reflective coating film including a hard coat layerformed by infiltration into a substrate and a low refractive index layercovering the hard coat layer was manufactured.

A cross-sectional image of the anti-reflective coating film is shown inFIG. 3( a), and a microscopic image of a part thereof is shown in FIG.3( b). As shown in FIG. 3, the anti-reflective coating film according toExample 1 was found to have a hard coat layer 2 (approximately 3.9 μm)including a binder cured by infiltration into a substrate 1 andinorganic nanoparticles dispersed in the binder; a low refractive indexlayer 3 (approximately 0.15 μm) including a binder cured on the hardcoat layer 2 and hollow particles 4 dispersed in the binder.

In addition, there was no separate layer between the hard coat layer 2and the low refractive index layer 3, and a ratio of the cross-sectionalarea of the hollow particles 4 to any cross-sectional area of the lowrefractive index layer 3 was approximately 90%, indicating that hollowparticles 4 were very compactly distributed in the low refractive indexlayer 3.

Example 2 Preparation of Anti-Reflective Coating Composition

Based on 100 parts by weight of a (meth)acrylate-based compoundcomprising 100 parts by weight of pentaerythritol hexaacrylate(molecular weight: 298.3), 11.33 parts by weight of fluorine-basedacrylate (product name: OPTOOL AR110, manufactured by DAIKIN, solidcontent: 15% by weight, methyl isobutyl ketone solvent), and 11.33 partsby weight of acrylate having a urethane functional group (manufacturedby KYOEISHA, product name: UA-306T, molecular weight: 1000);

approximately 15.87 parts by weight of silica nanoparticle-dispersedsilica sol (dispersion medium: methyl isobutyl ketone and methylalcohol, solid content: 40% by weight, number average diameter of silicananoparticles: 10 nm, manufactured by Gaematech, product name: Purisol);

approximately 11.33 parts by weight of a hollow silica-dispersedcolloidal solution (dispersion medium: methyl isobutyl ketone, solidcontent: 20% by weight, number average diameter of hollow silica: 50 nm,manufactured by Catalysts & Chemicals Industries Co., product name:MIBK-sol);

approximately 10.85 parts by weight of a photoinitiator (specifically,approximately 1.11 parts by weight of Darocur-1173, approximately 6.48parts by weight of Irgacure-184, approximately 2.15 parts by weight ofIrgacure-819 and approximately 1.11 parts by weight of Irgacure-907);and

approximately 251.85 parts by weight of a solvent (specifically,approximately 179.63 parts by weight of methyl ethyl ketone (MEK),approximately 24.07 parts by weight of ethanol, approximately 24.07parts by weight of n-butyl alcohol and approximately 24.07 parts byweight of acetyl acetone) were mixed to prepare an anti-reflectivecoating composition.

(Manufacturing of Anti-Reflective Coating Film)

An anti-reflective coating film was manufactured under the sameconditions and in the same manner as in Example 1, except using theabove anti-reflective coating composition.

A cross-sectional image of the anti-reflective coating film is shown inFIG. 4( a), and a microscopic image of a part thereof is shown in FIG.4( b). The anti-reflective coating film according to Example 2 was foundto have a hard coat layer 2 (approximately 2.8 μm) including a bindercured by infiltration into a substrate 1 and inorganic nanoparticlesdispersed in the binder; a low refractive index layer 3 (approximately0.145 μm) including a binder cured on the hard coat layer 2 and hollowparticles 4 dispersed in the binder.

In addition, there was no separate layer between the hard coat layer 2and the low refractive index layer 3, and a ratio of the cross-sectionalarea of the hollow particles 4 to any cross-sectional area of the lowrefractive index layer 3 was approximately 90%, indicating that hollowparticles 4 were very compactly distributed in the low refractive indexlayer 3.

In the anti-reflective coating film according to Example 2, inparticular, fluorine-based acrylate was comprised in the low refractiveindex layer, and thus phase separation of the composition effectivelyoccurred, and scratch resistance was also improved.

Example 3 Preparation of Anti-Reflective Coating Composition

Based on 100 parts by weight of a (meth)acrylate-based compoundcomprising 100 parts by weight of pentaerythritol hexaacrylate(molecular weight: 298.3) and 11.33 parts by weight of acrylate having aurethane functional group (manufactured by KYOEISHA, product name: 510H,molecular weight 2000);

approximately 15.87 parts by weight of silica nanoparticle-dispersedsilica sol (dispersion medium: methyl isobutyl ketone and methylalcohol, solid content: 40% by weight, number average diameter of silicananoparticles: 10 nm, manufactured by Gaematech, product name: Purisol);

approximately 11.33 parts by weight of a hollow silica-dispersedcolloidal solution (dispersion medium: methyl isobutyl ketone, solidcontent: 20% by weight, number average diameter of hollow silica: 50 nm,manufactured by Catalysts & Chemicals Industries Co., product name:MIBK-sol);

approximately 10.85 parts by weight of a photoinitiator (specifically,approximately 1.11 parts by weight of Darocur-1173, approximately 6.48parts by weight of Irgacure-184, approximately 2.15 parts by weight ofIrgacure-819 and approximately 1.11 parts by weight of Irgacure-907);and

approximately 251.85 parts by weight of a solvent (specifically,approximately 179.63 parts by weight of methyl ethyl ketone (MEK),approximately 24.07 parts by weight of ethanol, approximately 24.07parts by weight of n-butyl alcohol and approximately 24.07 parts byweight of acetyl acetone) were mixed to prepare an anti-reflectivecoating composition.

(Manufacturing of Anti-Reflective Coating Film)

The anti-reflective coating composition was applied to a triacetatecellulose film (thickness of 80 μm) using a wire bar (No. 9). The filmwas dried in a 90° C. oven for 1 minute, and then UV energy of 200mJ/cm² was irradiated thereto for 5 seconds to cure the composition.

Finally, an anti-reflective coating film including a hard coat layerformed by infiltration into a substrate and a low refractive index layercovering the hard coat layer was manufactured.

A cross-sectional image of the anti-reflective coating film wasvisualized by SEM. As a result, the anti-reflective coating filmaccording to Example 3 was found to have a hard coat layer(approximately 3.1 μm) including a binder cured by infiltration into asubstrate and inorganic nanoparticles dispersed in the binder; a lowrefractive index layer (approximately 0.16 μm) including a binder curedon the hard coat layer and hollow particles dispersed in the binder.

In addition, there was no separate layer between the hard coat layer andthe low refractive index layer, and a ratio of the cross-sectional areaof the hollow particles to any cross-sectional area of the lowrefractive index layer was approximately 90%, indicating that hollowparticles were very compactly distributed in the low refractive indexlayer.

Example 4 Preparation of Anti-Reflective Coating Composition

Based on 100 parts by weight of a (meth)acrylate-based compoundcomprising 100 parts by weight of pentaerythritol hexaacrylate(molecular weight: 298.3) and 11.33 parts by weight of acrylate havingan ester functional group (manufactured by SK Cytec, product name: DPHA,molecular weight: 524);

approximately 15.87 parts by weight of silica nanoparticle-dispersedsilica sol (dispersion medium: methyl isobutyl ketone and methylalcohol, solid content: 40% by weight, number average diameter of silicananoparticles: 10 nm, manufactured by Gaematech, product name: Purisol);

approximately 11.33 parts by weight of a hollow silica-dispersedcolloidal solution (dispersion medium: methyl isobutyl ketone, solidcontent: 20% by weight, number average diameter of hollow silica: 50 nm,manufactured by Catalysts & Chemicals Industries Co., product name:MIBK-sol);

approximately 10.85 parts by weight of a photoinitiator (specifically,approximately 1.11 parts by weight of Darocur-1173, approximately 6.48parts by weight of Irgacure-184, approximately 2.15 parts by weight ofIrgacure-819 and approximately 1.11 parts by weight of Irgacure-907);and

approximately 251.85 parts by weight of a solvent (specifically,approximately 179.63 parts by weight of methyl ethyl ketone (MEK),approximately 24.07 parts by weight of ethanol, approximately 24.07parts by weight of n-butyl alcohol and approximately 24.07 parts byweight of acetyl acetone) were mixed to prepare an anti-reflectivecoating composition.

(Manufacturing of Anti-Reflective Coating Film)

The anti-reflective coating composition was applied to a triacetatecellulose film (thickness of 80 μm) using a wire bar (No. 9). The filmwas dried in a 90° C. oven for 1 minute, and then UV energy of 200mJ/cm² was irradiated thereto for 5 seconds to cure the composition.

Finally, an anti-reflective coating film including a hard coat layerformed by infiltration into a substrate and a low refractive index layercovering the hard coat layer was manufactured.

A cross-sectional image of the anti-reflective coating film is shown inFIG. 5( a), and a microscopic image of a part thereof is shown in FIG.5( b). As shown in FIG. 5, the anti-reflective coating film according toExample 4 was found to have a hard coat layer 2 (approximately 2.78 μm)including a binder cured by infiltration into a substrate 1 andinorganic nanoparticles dispersed in the binder; a low refractive indexlayer 3 (approximately 0.18 μm) including a binder cured on the hardcoat layer 2 and hollow particles 4 dispersed in the binder.

In addition, there was no separate layer between the hard coat layer 2and the low refractive index layer 3, and a ratio of the cross-sectionalarea of the hollow particles 4 to any cross-sectional area of the lowrefractive index layer 3 was approximately 90%, indicating that hollowparticles 4 were very compactly distributed in the low refractive indexlayer 3.

Comparative Example 1 Preparation of Anti-Reflective Coating Composition

Based on 100 parts by weight of pentaerythritol hexaacrylate (PETA);

15.87 parts by weight of silica nanoparticle-dispersed silica sol(dispersion medium: methyl isobutyl ketone and methyl alcohol, solidcontent: 40% by weight, number average diameter: 10 nm, manufactured byGaematech, product name: Purisol);

approximately 11.33 parts by weight of a hollow silica-dispersedcolloidal solution (dispersion medium: methyl isobutyl ketone, solidcontent: 20% by weight, number average diameter of hollow silica: 50 nm,manufactured by Catalysts & Chemicals Industries Co., product name:MIBK-sol);

approximately 10.85 parts by weight of a photoinitiator (specifically,approximately 1.11 parts by weight of Darocur-1173, approximately 6.48parts by weight of Irgacure-184, approximately 2.15 parts by weight ofIrgacure-819 and approximately 1.11 parts by weight of Irgacure-907);and

approximately 251.85 parts by weight of a solvent (specifically,approximately 125.91 parts by weight of methyl isobutyl ketone,approximately 41.98 parts by weight of ethanol, approximately 41.98parts by weight of n-butyl alcohol and approximately 41.98 parts byweight of acetyl acetone) were mixed to prepare an anti-reflectivecoating composition.

(Manufacturing of Anti-Reflective Coating Film)

An anti-reflective coating film was manufactured under the sameconditions and in the same manner as in Example 1, except using theabove anti-reflective coating composition. A cross-sectional image ofthe anti-reflective coating film is shown in FIG. 6( a), and amicroscopic image of a part thereof is shown in FIG. 6( b).

As shown in FIG. 6, in the anti-reflective coating film according toComparative Example 1, phase separation of the composition did not occurproperly (see the circle of FIG. 6( a)), and in particular, hollowparticles 4 were very sparsely distributed in the low refractive indexlayer (see the circle of FIG. 6( b)). Thus, appearance of the filmbecame opaque, and scratch resistance and anti-reflective effect werealso reduced (see Experimental Example). In the anti-reflective coatingfilm of Comparative Example 1, a ratio of the cross-sectional area ofthe hollow particles to any cross-sectional area in the entire area ofthe hollow particle-distributed region was found to be approximately30˜60%.

Experimental Example

The anti-reflective coating films manufactured by Examples andComparative Example were evaluated for the following items, and theresults are shown in the following Table 1.

1) Measurement of reflectance: the back side of the anti-reflectivecoating film was treated with black color, and then low reflectionproperty was evaluated by minimum reflectance value. At this time, aShimadzu Solid Spec. 3700 spectrophotometer was used for measurement.

2) Measurement of transmittance and haze: HR-100 (Murakami Co., Japan)was used to evaluate transmittance and haze.

3) Evaluation of scratch resistance: the anti-reflective coating filmwas rubbed using a steel wool with a load of 500 g/cm² at a speed of 24m/min 10 times, and then the number of scratches having a length of 1 cmor longer was counted on the surface. At this time, when no scratch wasfound on the film surface, it was evaluated as “very excellent” (⊚), andwhen the numbers of scratch having a length of 1 cm or longer were 1 ormore to less than 5, 5 or more to less than 15, and 15 or more, each wasevaluated as “excellent” (◯), “moderate” (Δ), and “poor” (X),respectively.

4) Microscopic imaging of cross-section of film: the cross-section ofeach film prepared by microtoming was observed using a TransmissionElectron Microscope (name: H-7650, manufactured by HITACHI).

5) Evaluation of adhesion: adhesion of each film was evaluated by across cut test (ASTM D-3359) using a Nichiban tape.

TABLE 1 Trans- Reflectance mittance Haze Scratch (%) (%) (%) resistanceAdhesion Example 1 1.2 95.8 0.3 ◯ 5B Example 2 1.2 95.8 0.2 ⊚ 5B Example3 1.67 95.2 0.3 ⊚ 5B Example 4 1.30 95.5 0.3 ⊚ 5B Comparative 2.0 94.00.7 Δ 2B Example 1

As shown in Table 1, the anti-reflective coating films according toExamples had lower reflectance and higher transmittance than the film ofComparative Example, and they exhibited excellent scratch resistance andadhesion.

1. An anti-reflective coating film, comprising: a first layer thatcomprises a first (meth)acrylate-based binder and inorganicnanoparticles in the first (meth)acrylate-based binder, and that hasinfiltrated into a substrate; and a second layer that comprises a second(meth)acrylate-based binder and hollow particles in the second(meth)acrylate-based binder, and that covers the first layer, wherein aratio of the cross-sectional area of the hollow particles to anycross-sectional area of the second layer is 70 to 95%.
 2. Theanti-reflective coating film according to claim 1, wherein the first(meth)acrylate-based binder comprises a crosslinked polymer of a(meth)acrylate-based compound having a molecular weight of less than600.
 3. The anti-reflective coating film according to claim 1, whereinthe second (meth)acrylate-based binder comprises a crosslinked copolymerof a (meth)acrylate-based compound having a molecular weight of lessthan 600 and a (meth)acrylate-based compound having a molecular weightof 600 to 100,000.
 4. The anti-reflective coating film according toclaim 2, wherein the first layer further comprises the region having thecrosslinked copolymer of the (meth)acrylate-based compound having amolecular weight of less than 600 and the (meth)acrylate-based compoundhaving a molecular weight of 600 to 100,000, in addition to the regionhaving the crosslinked polymer.
 5. The anti-reflective coating filmaccording to claim 1, wherein the second layer further comprisesinorganic nanoparticles.
 6. The anti-reflective coating film accordingto claim 4, wherein the region having the crosslinked copolymer islocated to a depth of approximately 5 to 50% of the first layer, basedon the interface between the first and second layers.
 7. Theanti-reflective coating film according to claim 3, wherein thecrosslinked copolymer is comprised to exhibit an increasing distributiongradient toward the second layer.
 8. The anti-reflective coating filmaccording to claim 2, wherein the (meth)acrylate-based compound having amolecular weight of less than 600 is one or more compounds selected fromthe group consisting of pentaerythritol tri(meth)acrylate,pentaerythritol tetra(meth)acrylate, dipentaerythritolhexa(meth)acrylate, trimethylenepropane tri(meth)acrylate, ethyleneglycol di(meth)acrylate, 9,9-bis[4-(2-acryloxyethoxy)phenyl]fluorene,bis(4-methacryloxythiophenyl)sulfide, and bis(4-vinylthiophenyl)sulfide.9. The anti-reflective coating film according to claim 1, wherein thesecond (meth)acrylate-based binder comprises the crosslinked copolymerof a (meth)acrylate-based compound having a molecular weight of lessthan 600, a (meth)acrylate-based compound having a molecular weight of600 to 100,000 and a fluorine-based (meth)acrylate compound.
 10. Theanti-reflective coating film according to claim 9, wherein thefluorine-based (meth)acrylate compound comprises one or more compoundsselected from the group consisting of the compounds of the followingChemical Formulae 1 to 5:

wherein R¹ is a hydrogen group or an alkyl group having 1 to 6 carbonatoms, a is an integer of 0 to 7, and b is an integer of 1 to 3;

wherein c is an integer of 1 to 10;

wherein d is an integer of 1 to 11;

wherein e is an integer of 1 to 5;

wherein f is an integer of 4 to
 10. 11. The anti-reflective coating filmaccording to claim 3, wherein the (meth)acrylate-based compound having amolecular weight of 600 to 100,000 comprises a compound having two ormore molecules of the (meth)acrylate-based compound having a molecularweight of less than 600 linked via a linker.
 12. The anti-reflectivecoating film according to claim 3, wherein the (meth)acrylate-basedcompound having a molecular weight of 600 to 100,000 comprises acompound having one or more substituents selected from the groupconsisting of an epoxy group, a hydroxyl group, a carboxyl group, athiol group, an aromatic or aliphatic hydrocarbon group having 6 carbonatoms or more, and an isocyanate group.
 13. The anti-reflective coatingfilm according to claim 11, wherein the linker comprises a urethanebond, a thioether bond, an ether bond or an ester bond.
 14. Theanti-reflective coating film according to claim 1, wherein the inorganicnanoparticles have a number average diameter of 5 to 50 nm.
 15. Theanti-reflective coating film according to claim 1, wherein the inorganicnanoparticles are silica nanoparticles.
 16. The anti-reflective coatingfilm according to claim 1, wherein the hollow particles have a numberaverage diameter of 5 to 80 nm.
 17. The anti-reflective coating filmaccording to claim 1, wherein the hollow particles are hollow silicaparticles.
 18. A phase-separated single-coat anti-reflective coatingfilm structure, comprising: a single-coating on a substrate, whereinsaid coating has a phase-separated structure comprising: a first layercomprising a first (meth)acrylate-based binder and inorganicnanoparticles in the first (meth)acrylate-based binder, said first layerhaving infiltrated into the substrate; and a second layer comprising asecond (meth)acrylate-based binder and hollow particles in the second(meth)acrylate-based binder, and covering the first layer, and wherein aratio of the cross-sectional area of the hollow particles to anycross-sectional area of the second layer is 70 to 95%.
 19. Ananti-reflective coating film structure, comprising: a substrate, a firstlayer comprising a first (meth)acrylate-based binder and inorganicnanoparticles in the first (meth)acrylate-based binder within saidsubstrate; and a second layer that includes comprising a second(meth)acrylate-based binder and hollow particles in the second(meth)acrylate-based binder, and covers covering the first layer,wherein a ratio of the cross-sectional area of the hollow particles toany cross-sectional area of the second layer is 70 to 95%, and whereinsaid first layer has infiltrated into said substrate.
 20. Theanti-reflective coating film structure of claim 19, wherein thestructure does not comprise a separate and distinctive layer comprisingonly a binder between the first layer and the substrate.
 21. Theanti-reflective coating film structure of claim 19, wherein thestructure does not comprise a separate and distinctive layer comprisingonly a binder between the first layer and the second layer.